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Gene transfer material of functionalized nano curcumin and preparation method

A technology of gene introduction and curcumin, which is applied in the direction of introducing foreign genetic material by using a carrier, recombinant DNA technology, etc., can solve the problems of limited penetrating power of the gene gun and unstable results, and achieve good biocompatibility and material dispersibility Good, easy-to-operate effect of preparation reaction

Inactive Publication Date: 2014-06-11
王深明 +2
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  • Abstract
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  • Application Information

AI Technical Summary

Problems solved by technology

Since there are many serious deficiencies in the viral gene transfer system, such as the possibility of activation of proto-oncogenes by viral transfection, the non-viral transfection method is currently a research hotspot. In the above-mentioned non-viral transfection, microinjection once Only one cell can be processed; the penetration of the gene gun is very limited; the results of the calcium phosphate co-precipitation method are unstable; only the cationic liposome method shows good transfection efficiency, but the high toxicity limits its application

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  • Gene transfer material of functionalized nano curcumin and preparation method
  • Gene transfer material of functionalized nano curcumin and preparation method
  • Gene transfer material of functionalized nano curcumin and preparation method

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Embodiment Construction

[0022] 1. Preparation of the gene transfer material of the present invention:

[0023] 1. Take materials: main materials: zinc chloride, analytically pure, product of Aldrich Company; curcumin, MW660, analytically pure, used without further purification steps, product of Aldrich Company. All preparative glassware were sonicated in ethanol for 5 minutes, then rinsed with double distilled water, and washed with washing solution H 2 0 / HNO 3 (65%) / H 2 o 2 (35%) (1:1:1, v / v / v) for cleaning, followed by double-distilled water and acetone for cleaning, and finally air-dried.

[0024] 2. Preparation of materials: Dissolve zinc chloride in deionized water to prepare 0.1 mmol / L, and dissolve curcumin in absolute alcohol to prepare 2 mmol / L fresh curcumin solution. First, add 1ml of 2mmol / L fresh curcumin solution to 0.1mmol / L zinc chloride solution, place it in a 25mL beaker, stir thoroughly for 30min, let it stand for 1 day, centrifuge at 8000r / m speed, and then use double distille...

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Abstract

The invention discloses a gene transfer material of functionalized nano curcumin, which is a composite material consisting of curcumin and zinc oxide and has average diameter of about 100nm, curcumin content of 97.77wt% and zinc ion content of 2.23wt% and forms a curcumin-Zn<2+> nano spherical material. The invention also discloses a preparation method of the gene transfer material of the functionalized nano curcumin. The gene transfer material disclosed by the invention has relatively high transfection efficiency which can reach about 40% in human breast cancer cells; the gene transfer material has low toxicity, the curcumin has good biocompatibility, and the cell survival rate is very high; the material has good dispersity and meets the transfection requirements; the cost is remarkably low; the preparation reaction of the materials is simple and easy to operate and has good repeatability; the gene transfer material has a good application prospect and can be applied to the preparation of anti-tumor drugs.

Description

[technical field] [0001] The invention relates to a high transfection efficiency and low cytotoxicity functionalized nano-curcumin gene introduction material and a preparation method. [Background technique] [0002] With the completion of the determination of the human gene map, our understanding of the pathogenesis of human diseases has made breakthrough progress at the genetic level. Current research shows that the occurrence and development of many diseases are closely related to genes. If the gene fragments or gene mutations specifically related to the disease can be screened out, specific treatments can be targeted at the gene level, such as by introducing related deletion genes or silencing genes to enhance related deletion functions or silence disease-causing genes , so as to achieve the purpose of complete treatment. Safely and effectively introducing target genes into organisms is the key and difficult point in this research field. [0003] Gene transfer systems ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12N15/85
Inventor 王深明张德元刘勇夏浩明周鸿雁李梓伦常光其徐安武
Owner 王深明